Literature DB >> 23064591

Location of periventricular nodular heterotopia is related to the malformation phenotype on MRI.

G González1, L Vedolin, B Barry, A Poduri, C Walsh, A J Barkovich.   

Abstract

BACKGROUND AND
PURPOSE: Periventricular nodular heterotopia are common malformations of cortical development that are associated with many clinical syndromes and with many different neuroimaging phenotypes. The purpose of this study was to determine whether specific malformation phenotypes may be related to location, side, or number of PNH as assessed by MR imaging.
MATERIALS AND METHODS: MR images of 200 patients previously diagnosed with PNH were retrospectively analyzed. PNH were classified according to their location along the ventricles (anterior, posterior, or diffuse), side (unilateral or bilateral), and number of nodules (<5, 6-10, or >10). The cerebrum, brain stem and cerebellum were analyzed to assess associated anomalies. Associations between PNH location and the presence of other anomalies were tested by using Fisher exact test and χ2 test.
RESULTS: Posterior PNH were significantly associated with malformations of the cerebral cortex, diminished white matter volume, and mid-/hindbrain anomalies. Diffuse PNH were associated with diminished white matter volume, callosal "anomalies," and the presence of megacisterna magna. Unilateral PNH were strongly associated with cortical malformations.
CONCLUSIONS: Certain malformation complexes are associated with PNH in specific locations: posterior PNH with cerebral cortical and mid-/hindbrain malformations and diffuse PNH with callosal anomalies and megacisterna magna. Knowledge of these associations should allow more directed analyses of brain MR imaging in patients with PNH. In addition, knowledge of these associations may help to direct studies to elucidate the causes of these malformation complexes.

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Year:  2012        PMID: 23064591      PMCID: PMC3951137          DOI: 10.3174/ajnr.A3312

Source DB:  PubMed          Journal:  AJNR Am J Neuroradiol        ISSN: 0195-6108            Impact factor:   3.825


  20 in total

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2.  Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations.

Authors:  E Parrini; A Ramazzotti; W B Dobyns; D Mei; F Moro; P Veggiotti; C Marini; E H Brilstra; B Dalla Bernardina; L Goodwin; A Bodell; M C Jones; M Nangeroni; S Palmeri; E Said; J W Sander; P Striano; Y Takahashi; L Van Maldergem; G Leonardi; M Wright; C A Walsh; R Guerrini
Journal:  Brain       Date:  2006-05-09       Impact factor: 13.501

3.  Anomalies of the corpus callosum: an MR analysis of the phenotypic spectrum of associated malformations.

Authors:  Steven W Hetts; Elliott H Sherr; Stephanie Chao; Sarah Gobuty; A James Barkovich
Journal:  AJR Am J Roentgenol       Date:  2006-11       Impact factor: 3.959

4.  Electroencephalographic recordings of focal seizures in patients affected by periventricular nodular heterotopia: role of the heterotopic nodules in the genesis of epileptic discharges.

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Review 10.  Malformations of cortical development and epilepsy.

Authors:  Richard J Leventer; Renzo Guerrini; William B Dobyns
Journal:  Dialogues Clin Neurosci       Date:  2008       Impact factor: 5.986

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  10 in total

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2.  Quantitative assessment of corpus callosum morphology in periventricular nodular heterotopia.

Authors:  Heath R Pardoe; Simone A Mandelstam; Rebecca Kucharsky Hiess; Ruben I Kuzniecky; Graeme D Jackson
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Review 3.  Fetal magnetic resonance imaging: supratentorial brain malformations.

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6.  Germline and somatic mutations in cortical malformations: Molecular defects in Argentinean patients with neuronal migration disorders.

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7.  The clinical and imaging features of FLNA positive and negative periventricular nodular heterotopia.

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8.  Whole-brain multimodal MRI phenotyping of periventricular nodular heterotopia.

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9.  Massive obesity and hyperphagia in posterior bilateral periventricular heterotopias: case report.

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10.  A Rare Cause of Refractory Epilepsy: Posterior Periventricular Nodular Heterotopia.

Authors:  Meltem C Direk; Mustafa Komur; Anıl Ozgur; Cetin Okuyaz
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  10 in total

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